Tekmen-Clark Merve, Gleason Evanna
Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA.
Vis Neurosci. 2013 May;30(3):91-103. doi: 10.1017/S0952523813000126. Epub 2013 May 30.
Nitric oxide (NO) is known to exert multiple effects on the function of many retinal neurons and their synapses. Therefore, it is equally important to understand the potential sources of NO within the retina. To explore this, we employ a combination of 4-amino-5-methylamino-2',7'-difluorofluorescein diacetate (DAF-FM) based NO detection and immunohistochemistry for the NO synthetic enzymes, neuronal and endothelial nitric oxide synthase (nNOS and eNOS). We find DAF signals in photoreceptors, horizontal cells, amacrine cells, efferent synapses, Müller cells, and cells in the ganglion cell layer (GCL). nNOS immunoreactivity was consistent with the DAF signal with the exception that horizontal cells and Müller cells were not clearly labeled. eNOS-like immunoreactivity (eNOS-LI) was more widespread with photoreceptors, horizontal cells, occasional bipolar cells, amacrine cells, Müller cells, and cells in the GCL all showing labeling. Double labeling with antibodies raised against calretinin, syntaxin, and glutamine synthetase confirmed that horizontal cells, amacrine cells, and Müller cells (respectively) were expressing eNOS-LI. Although little or no nNOS labeling is observed in horizontal cells or Müller cells, the expression of eNOS-LI is consistent with the ability of these cells to produce NO. Together these results suggest that the capability to produce NO is widespread in the chicken retina. We propose that multiple forms of regulation for nNOS and eNOS play a role in the patterning of NO production in the chicken retina.
已知一氧化氮(NO)对许多视网膜神经元及其突触的功能具有多种作用。因此,了解视网膜内NO的潜在来源同样重要。为了探究这一点,我们采用了基于4-氨基-5-甲基氨基-2',7'-二氟荧光素二乙酸酯(DAF-FM)的NO检测方法与针对NO合成酶、神经元型和内皮型一氧化氮合酶(nNOS和eNOS)的免疫组织化学方法相结合。我们在光感受器、水平细胞、无长突细胞、传出突触、穆勒细胞以及神经节细胞层(GCL)中的细胞中发现了DAF信号。nNOS免疫反应性与DAF信号一致,但水平细胞和穆勒细胞未被清晰标记。eNOS样免疫反应性(eNOS-LI)分布更广泛,光感受器、水平细胞、偶尔的双极细胞、无长突细胞、穆勒细胞以及GCL中的细胞均显示有标记。用针对钙视网膜蛋白、 syntaxin和谷氨酰胺合成酶的抗体进行双重标记证实,水平细胞、无长突细胞和穆勒细胞(分别)表达eNOS-LI。尽管在水平细胞或穆勒细胞中观察到很少或没有nNOS标记,但eNOS-LI的表达与这些细胞产生NO的能力一致。这些结果共同表明,产生NO的能力在鸡视网膜中广泛存在。我们提出,nNOS和eNOS的多种调节形式在鸡视网膜中NO产生的模式形成中起作用。